Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New <i>ABCA4</i> Mutations.

Falfoul, Yousra; Habibi, Imen; Turki, Ahmed; Chebil, Ahmed; Hassairi, Asma; Schorderet, Daniel F; El Matri, Leila

Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations.

Falfoul, Yousra; Habibi, Imen; Turki, Ahmed; Chebil, Ahmed; Hassairi, Asma; Schorderet, Daniel F; El Matri, Leila.

Afiliación

Falfoul Y; Hedi Rais Institute of Ophthalmology (Department B), Tunis, Tunisia.
Habibi I; Oculogenetic Laboratory LR14SP01, Tunis, Tunisia.
Turki A; Institute for Research in Ophthalmology (IRO), Sion, Switzerland.
Chebil A; Oculogenetic Laboratory LR14SP01, Tunis, Tunisia.
Hassairi A; Hedi Rais Institute of Ophthalmology (Department B), Tunis, Tunisia.
Schorderet DF; Oculogenetic Laboratory LR14SP01, Tunis, Tunisia.
El Matri L; Hedi Rais Institute of Ophthalmology (Department B), Tunis, Tunisia.

J Ophthalmol ; 2018: 1030184, 2018.

Article en En | MEDLINE | ID: mdl-29736279

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Ophthalmol Año: 2018 Tipo del documento: Article País de afiliación: Túnez